3,5-diketals of 4,5 - seco-gonane-3,5,17-triones and process of preparation

ABSTRACT

WHEREIN R&#34; IS LOWER ALKYL AND R&#34;&#39;&#39; IS SELECTED FROM THE GROUP CONSISTING OF LOWER ALKYLENE AND SUBSTITUTED LOWER ALKYLENE; AND A IS SELECTED FROM THE GROUP CONSISTING OF TWO HYDROGENS AND A DOUBLE BOND THESE COMPOUNDS ARE USEFUL AS INTERMEDIATES IN THE TOTAL SYNTHESIS OF STEROIDS, PARTICULARLY THOSE HAVING SUBSTITUENTS ON THE 17 CARBON ATOM.   =C(-O-R&#34;)2 AND =C&lt;(-O-R&#34;&#39;&#39;-O-)   WHREIN R&#39;&#39; REPRESENTS AN ALKYL HAVING FROM 1 TO 4 CARBON ATOMS; X REPRESENTS A MEMBER SELECTED FROM THE GROUP CONSISTING OF   X AND THE 9,11-POSITION IS A   3-(X=),13-R&#39;&#39;-GON-4-EN-17-ONE WHERE C-4 IS REPLACED BY   THE PRESENT INVENTON RELATES TO 3,5-DIKETALS OF 4,5SECO-GONANE-3,517-TRIONES OF THE FORMULA

United States Patent Int. Cl. C07d 13/04 US. Cl. 260--340.9 4 Claims ABSTRACT OF THE DISCLOSURE The present invention relates to 3,5-diketals of 4,5- seco-gonane-3,5,17-triones of the formula wherein R represents an alkyl having from 1 to 4 carbon atoms; X represents a member selected from the group consisting of wherein R" is lower alkyl and R is selected from the group consisting of lower alkylene and substituted lower alkylene; and A is selected from the group consisting of two hydrogens and a double bond. These compounds are useful as intermediates in the total synthesis of steroids, particularly those having substituents on the 17 carbon atom.

THE PRIOR ART It is a well known fact that the preparation of 19-nor steroids substituted in the 17 position presents diflicult problems due to the presence of the functions on the steroid molecule apt to be attacked at the very moment of the introduction of the desired substituent in the 17 position. This is the case, in particular, with steroids having a ketone function in the 3 position and/or double bond in the 4,5 position.

Moreover, it is known that in the former processes for the preparation of steroid derivatives by means of total synthesis, the authors have, as a rule, preferred to complete the construction of the steroid skeleton first, and only then to proceed with the substitution in the 17 position (see, for example, Velluz et a1., Recent Advances in the Total Synthesis of Steroids, Angew. Chem. Intern, Edit., vol. 4 [1965] No. 3).

OBJECTS OF THE INVENTION An object of the present invention is the obtention of a steroid intermediate which can undergo substitution in the 17 position and thereafter total synthesis steps to form a steroid substituted in the 17 position.

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Another object of the present invention is the obtention of 3,5-diketals of 4,5-seco-gonane-3,5,17-triones of the formula wherein R represents an alkyl having from 1 to 4 carbon atoms; X represents a member selected from the group consisting of O and wherein R is a member selected from the group consisting of hydrogen and the acyl of an organic carboxylic acid having from 1 to 18 carbon atoms, R is an alkyl having from 1 to 4 carbon atoms, Z is a member selected from the group consisting of oxygen,

wherein R" is lower alkyl and R' is selected from the group consisting of lower alkylene and substituted lower alkylene, and A is selected from the group consisting of two hydrogens and a double bond, with a ketalization agent under ketalizing conditions, saponifying the resultant 3,5-diketals, of 4,5-seco-gonane-3,S-diones of the formula where X is a member selected from the group consisting of OR O\ and R" wherein R" and R have the above-assigned meanings, R and A have the above-assigned meanings, and R is the acyl of an organic carboxylic acid having from 1 to 18 carbon atoms, by the action of an alkaline saponifying agent, oxidizing the resultant 3,5-diketals of 4,5-sec0- gonane-l7fi-ol-3,5-diones of the formula wherein R, X and A have the above-assigned meanings by the action of an hydroxyl oxidizing agent, and recovering said 3,5-diketals of 4,5-seco-gonane-3,5,17-triones.

A further object of the present invention is the obtention of the novel intermediate 3,5-diketals of 4,5-secogonane-3,5-diones of the formula where R is selected from the group consisting of hydrogen and the acyl of an organic carboxylic acid having from 1 to 18 carbon atoms, R is alkyl having from 1 to 4 carbon atoms, X is selected from the group consisting of DESCRIPTION OF THE INVENTION It has now been discovered that a novel class of intermediate products for the synthesis of steroid derivatives, namely, the 3,5-diketals of 13fl-alkyl-4,5-seco-gonane-3,5,17-triones of the general formula given in the above, permit, in contrast to the 3-monoketals already known, to bypass the difficulties previously met with in the preparation of 19-nor steroids substituted in the 17 position, due to the possibility of introducing at this stage the desired substituents in the 17 position.

The 3,5-diketals of the 13,3-alkyl-4,5-seco-gonane-3,5, 17-triones thus formed show in neutral or alkaline medium an excellent stability with regard to the functions in the 3 and positions, which facilitates the possible conversions in the 17 position. Moreover, they are, after splitting of the ketal functions in the 3 and 5 positions, easily cyclized by the usual agents to give the tetracyclic steroid skeleton.

The present invention relates to a new class of intermediate produc s or the synthesis of steroid derivatives 4 as well as to a process for the preparation of these products.

More particularly, the invention relates to the 3,5-diketals of the 13fl-alkyl-4,5-seco-gonane 3,5,l7-triones of the general Formula I wherein, here and in the following, R is an alkyl radical containing 1 to 4 carbon atoms, X represents the group R" being a lower alkyl, or X represents the group O RHI R' being a lower alkylene radical, substituted or unsubstituted, and the dashed line represents a possible 9(11) double bond.

The process for the preparation of the compounds of the general Formula I, also object of the present invention, is characterized in that a 3-Z-13fl-alkyl-17p-OR-4,5- seco-gonane-S-one of the general Formula II Z o II wherein Z represents a ketone oxygen or X, R and X having the above assigned meanings, R is hydrogen or the acyl radical of an organic carboxylic acid having 1 to 18 carbon atoms, and the dashed line represents a possible 9( 10) double bond, is subjected to the action of a ketalization agent, the diketal obtained, of the general Formula III wherein X, -R, R and the dashed line have the boveassigned meanings, when -R represents the radical of an organic carboxylic acid having from 1 to 18 carbon atoms, is saponified, and the diketal of the general Formula IV wherein X, R and the dashed line have the above-assigned meanings, is reacted with an oxidizing agent, and the desired 3,5-diketal of 13p-alkyl-4,5-seco-gonane-3,5, 17-trione is isolated,

The process, also object of the invention, can be ad vantageously executed as follows:

(A) The ketalization agent is chosen from the group consisting of the lower cyclic ketals, the lower non-cyclic ketals and the lower alkanols. The work is conducted in the presence of an acid catalyst.

(B) The cyclic ketals are chosen from the group consisting of Z-methyl-Z-ethyl-dioxolane, 2-rnethyl-2-phenyldioxolane, 2-methyl-4-(6-methylbenzyl)-dioxolane, 2,2- dimethyl-4-(6-methylbenzyl)-dioxolane, 2 chloromethyldioxolane, 2-(B-chloro)-ethyl-dioxolane and 2-(/3-bromo)- ethyl-dioxolane.

(C) The non-cyclic ketals are selected from the group consisting of the dimethyl ketal of acetone, the diethyl ketal of acetone, the dimethyl ketal of Z-butanone, the dimethyl ketal of dimethylformamide and the diethyl ketal of dimethylformamide.

(D) The aliphatic alcohols employed as ketalizing agents are chosen from the group consisting of glycols such as lower alkanediols, for example, ethyleneglycol, 1,3- propanediol, 2,2-dimethyl-1,3-propanediol, and of lower alkanols such as methanol or ethanol.

(E) the saponification of the 3,5-diketal of l3fl-alkyll7B-acyloxy-4,5-seco-gonane-3,S-dione of the general Formula III is effected by an alkaline agent such as an alkali metal hydroxide, for example, sodium or potassium hydroxide. The work is carried out in a lower alkanol such as methanol or ethanol.

(F) The oxidation of the hydroxyl in the 17 position is realized according to the Oppenauer method by means of a lower aliphatic ketone such as lower alkanones, for example, acetone, methylethyl ketone, methylisobutyl ketone or lower cycloalkanones, for example, cyclohexanone, in the presence of an aluminum tertiary lower al kanolate such as aluminum isopropylate.

(G) The oxidation of the hydroxyl in the 17 position is effected by using, as oxidizing agent, chromic acid anhydride in pyridine.

As it has already been mentioned, the advantages of the novel compounds of the general Formula I lie in particular in the fact that they allow an easy preparation of 19-nor steroids substituted in the 17 position, as it will be explained in the following.

The introduction of a substituent in the 17m position is realized, for example, by reaction of a compound of Formula I with an organometallic compound of the type R Li or R MgX (X being a halogen and, in particular, bromine or iodine and R represents a hydrocarbon radical, preferably lower alkyl, lower alkenyl or lower alkynyl).

In the particular case of ethynylation, this reaction may be realized with the aid of an ethynyl magnesium halide or also with the aid of an alkali metal acetylide or also with the aid of acetylene while operating in the presence of tertiary alcoholates or amides of alkali metals or alkaline earth metals.

The introduction of the ethyl or vinyl radical in the 170: position can be effected with excellent yields in an indirect fashion in two steps. By ethynylation of the ketone in the 17 position and subsequent reduction of the ethynyl radical by hydrogenation in the presence of a catalyst having a platinum or palladium base, the 17a-ethyl derivative is obtained, Whereas if the reduction is arrested after the absorption of a mol equivalent of hydrogen gas, the 17avinyl derivative is obtained.

The process of indirect introduction may furthermore be significant with regard to the preparation of the 17mpropyl derivatives. In that case, allyl magnesium bromide can be reacted with a compound of Formula I, then the resultant allylic derivative is subjected to a hydrogenation in the presence of a catalyst having a platinum or palladium base.

The 3,5-diketals of the 13,6-alkyl-17u-R -17B-hydroxy- 4,5-seco-gonane-3,S-diones, possibly having a double bond in the 9(11) position, obtained by the above reactions,

6 can be esterified in the 17 position with an organic carboxylic acid having from 1 to 18 carbon atoms by employing the usual acylation agents such as the corresponding acid, its anhydride or its chloride.

Such acids are the aliphatic or cycloaliphatic carboxylic acids, saturated or unsaturated, or the aromatic or heterocyclic carboxylic acids, for example, the alkanoic acids such as formic, acetic, propionic, butyric, isobutyric, valeric, isovaleric, trimethylacetic, caproic, fi-trimethylpropionic, enanthic, caprylic, pelargonic, capric, undecylic, lauric, myristic, palmitic, stearic, etc., the alkenoic acids such as undecylenic, oleic, etc., the cyclo alkyl carboxylic acids such as cyclopentyl-, cyclopropyl-, cyclobutyland cyclohexyl-carboxylic acids, the cycloalkylalkanoic acids such as cyclopropylmethyl carboxylic acid, cyclobutylmethyl carboxylic acid, cyclopentylethyl carboxylic acid, cyclohexylethyl carboxylic acid, the cyclopentylacetic, cyclohexylacetic, or propionic acids, the phenylalkanoic acids such as phenylacetic or propionic acids, benzoic acid, the phenoxyalkanoic acids such as phenoxy acids, p-chlorophenoxyacetic acid, 2,4-dichlorophenoxyacetic acid, 4- tert.-butyl-phenoxyacetic acid, 3-phenoxypropionic acid, 4-phenoxybutyric acid, the furane Z-carboxylic acids such as S-tert.-butylfurane-Z-carboxylic acid, S-bromo-furane- 2-carboxylic acid, the nicotinic acids, the fi-ketoalkanoic acids, for example, the acetylacetic, propionylacetic, butyrylacetic acids, etc.

The 3,5-diketals of the 13fi-R'-l7ut-R 17,B-hydroxy- 4,5-seco-gonane-3,S-diones with or without a 9(11) double bond, whether esterified or unesterified in the 176 position, can be subsequently converted into tetracyclic steroids.

For that purpose, such a 3,5-diketal of a 13B-R'-170c R -l7 3-hydroxyor 17,8-acyloxy4,S-seco-gonane-3,5-dione formed as indicated above is subjected to a ketal hydrolysis in the presence of an acid, such as citric, acetic, hydrochloric or sulfuric acid, and in the presence of one or several solvents such as an alcohol, for example, the methanol or ethanol, and a hydrocarbon such as benzene or toluene. In this manner the ketones in the 3 and 5 positions are regenerated and the corresponding 3,5-dioxo derivative is recovered possibly having a double bond in the 9(10) position. Next, this 3,5-dioxo derivative is subjected to the action of a basic cyclization agent such as an alkali metal alcoholate, or to the action of an acid cyclization agent such as hydrochloric acid or the hydrochloric acid-acetic acid mixture.

Thus, a tetracyclic steroid of the general formula wherein R, R and R have the previous meanings, is obtained, possibly with a double bond in the 9(10) position.

In the case where the cyclization agent is a secondary base such as, for example, pyrrolidine, the correpsonding enamines are obtained in the 3-position, which by means of acid hydrolysis supply the above-indicated 3- oxo-A or 3-oxo-A derivatives.

By applying the methods described in the preceding, it is possible to prepare, starting with the compounds of the general Formula I, physiologically active steroids such as, for example, 17a-ethynyl-19-nor-testostterone, 17aethyl-l9-nor-testosterone, the acetate of l7a-ethyny1-l9- nor-testosterone, 17a-ethynyl-M- -estradiene-17,6-01-3-one, 13fl-ethyl-17at-ethynyl-A -gonene-17,8-01-3-one, 13,8,17ot-diethyl-n -gonene-l7fi-0l-3-one, l3 8-ethyl-17a-ethynyl-A gonadiene-l75-ol-3-one and the corresponding 13,8-n-pro pyl and 13fi-n-butyl derivatives.

As it has been shown in the preceding, tetracyclic steroids of gonanic structure can be prepared by starting with the compounds of Formula I. It is also possible to obtain by starting with the said compounds of Formula I, tetracyclic steroids of pregnanic structure having also a considerable physiological activity. Thus, for example, 16a,17a-dihydroxy-19-nor-progesterone and its condensation derivatives with carbonyl compounds can be prepared by means of a process starting from the 3,5-diketals of the general Formula I. The advantages of the new process will become evident by the following.

US. Pat. No. 3,243,433 describes a process for the preparation of 16a,17a-dihydroxy-19-nor-progesterone starting from 3-methoxy-16a,17a-isopropylidenedioxy-19- nor-A -pregnatriene-2O=0l. This process comprises four distinct operation steps.

The 3 methoxy-16a,17a-isopropylidenedioxy-l9-nor- A -pregnatriene-ZO-ol is prepared according to the process described in US. Pat. No. 3,077,471, starting from 16a,17a-isopropylidenedioxy-progesterone, also in a process of four steps. One of these steps consists in demethylating in the position a 1,4-dienic derivative of pregnane, which is thus converted into a derivative with an aromatic A ring. This demethylation is effected by pyrolysis at a temperature of 600 C.

Finally, 16a,17a-isopropylidenodioxy-progesterone is obtained, for example, by means of oxidation of 16- dehydro-progesterone (see US. Pat. No. 3,165,541 and French Pat. No. 1,158,850) which itself is prepared by starting with natural products such as the sapogenins (see US. Pat. No. 2,420,489) or progesterone (Pelman et al., J. Am. Chem. Soc. 74, 2126 [1952]).

The obtention of 16a,17a-dihydroxy-19-nor-progesterone, according to the processes mentioned above, is consequently lengthy and its overall yield is poor. Eight stages are actually necessary to obtain 16a,l7a-dihyroxy- 19-nor-progesterone, starting with 16a,17a-isopropylidenedioxy-A -pregnene-3,20-dione, the preparation of which, starting from the sapogenins or progesterone, required supplementary steps.

Therefore, the process for the preparation of l6cx,17ocdihydroxy-l9-nor-progesterone and its condensation derivatives with carbonyl compounds, having been elaborated due to the utilization of a 3,5-diketal of the general Formula I as a starting compound, is advantageous from more than one viewpoint.

The said process is realized as follows:

In a basic medium, an alkali metal cyanide is reacted in the presence of an organic acid, preferably an alkanoic acid, on 3,5-bis-(ethylenedioxy)-4,5-seco-estrane-17-one, thus obtaining a mixture of isomeric cyanohydrin, rich in 3,5-bis-(ethylenedioxy)-17fi-cyano-4,5-seco-estrane-17aol, which is then dehydrated by the action of an acid dehydrating agent in a polar solvent to obtain 3,5-bis- (ethylenedioxy)-17-cyano-4,5-seco-A -estrene, on which methyl lithium or a methyl magnesium halide is reacted to form intermediately 3,5-bis-(ethylened-ioxy)-20imino- 4,5-sec-19-nor-A -pregnene. The hydrolysis of this product, effected in the presence of an acidic agent such as a lower alkanoic acid, leads to 4,5-seco-19-nor-A -pregnene-3,5,20-trione. This product is then cyclized by the action of a secondary amine to obtain the enamine in the 3 position of 19-nor-A -pregnadiene-3,20-dione. This latter compound is subjected to the action of an acid agent, such as a mineral acid to form the corresponding imonium salt, which is then hydrolyzed in situ by the action of a basic agent, such as an aqueous alkali metal hydroxide, thus obtaining 19-nor-A -pregnadiene-3,20- dione. This compound, by the action of a hydroxylating agent, which acts on the 16(17) double bond, supplies 19-nor-A -pregnene-1'6a,17a-diol-3,20-dione, which is condensed either with an aldehyde or ketone as desired.

In comparison with the process described in the preceding, corresponding, in particular, to US. Pats. Nos. 3,243,433 and 3,077,471, the new process possesses the advantage of making possible the access to :,l7a-dihydroxy-19-nor-progesterone and its condensation derivatives with carbonyl compounds by means of total synthesis. It follows therefrom that the process of demethylation in the 10 position of the pregnane derivatives, always a difficult and onerous task, is thus avoided and that the process is relatively brief. Only six operational steps are actually needed to arrive at 16a,17a-dihydroxy-19-n0r progesterone starting with 3,5-bis-(ethylenedioxy)-4,5- seco-seco-estrane-l7-one.

In the above process for the production of 160:,17a-dihydroxy-l9-nor-progesterone and its condensation derivatives with carbonyl compounds, it is preferable to utilize the following operatory steps:

(A) In the preparation of the cyanohydrin, the alkali metal cyanide is potassium cyanide or sodium cyanide. The lower alkanoic acid utilized is acetic or propionic acid. It is also preferable to operate in the presence of a polar organic solvent, preferably a lower alkanol such as ethanol or methanol. In order to obtain the 17,8-cyano- 17a-hydroxylated derivative in preponderance, it is advisable to utilize a basic media and a deficiency of the organic acid with respect to the amount of alkali metal cyanide utilized.

(B) The desired 17a-hydroxylated epimer is separated by fractional crystallization from an aliphatic ether such as ethyl ether. The 17/3-hydroxylated epimer is recovered from the mother liquor and converted to the starting compound by action of a strong base.

(C) The acid dehydrating agent utilized for the dehydrating of 3,5-bis-(ethylenedioxy)-17B-cyano-4,5-secoestrane-17a-ol is, for example, thionyl chloride, phosphorus oxychloride, methanesulfonyl chloride, etc. The polar solvent utilized is preferably a cyclic tertiary amine such as pyridine or methylethyl pyridine. An excess of the acid dehydrating agent is utilized and the reaction is advantageously effected at room temperature.

(D) The methylation with methyl lithium or methyl magnesium halide is conducted in the presence of an aliphatic or cyclic ether such as ethyl ether or tetrahydrofurane. The cyano derivative is solubilized in a solvent such as benzene. The imino compound obtained is not isolated and is hydrolyzed at the same time as the ketal functions by the addition to the reaction medium of a lower alkanoic acid such as acetic or propionic acid.

(E) The secondary amine utilized as a cyclization agent is preferably pyrrolidine or a substituted pyrrolidine and the reaction takes place preferably in the presence of a polar organic solvent, for example, a lower alkanol such as ethanol or methanol.

(F) The mineral acid employed for the formation of the immonium salt is preferably sulfuric or hydrochloric acid in an aqueous medium. The immonium salt is not isolated and is hydrolyzed by the action of an aqueous alkali metal hydroxide such as sodium hydroxide or potassium hydroxide.

(G) The hydroxylating agent which acts on the 16( 17) double bond is advantageously potassium permanganate or osmium tetraoxide.

(H) The 16a,17a-dihydroxy 19 nor-progesterone can be easily condensed with a carbonyl compound such as an aldehyde or a ketone while operating in the presence of a strong mineral acid such as perchloric acid. If acetone is utilized under these conditions, 16a,17a-isopropylidenedioxy 19 nor-progesterone is obtained, whereas when acetophenone is employed, 16a,17a-(phenylethylenedioxy)-19-nor-progesterone is obtained.

The starting compounds of the process of the invention are described and are accessible by application of the processes of French Patents Nos. 1,243,000, 1,364,556, 1,476,509 and 1,432,569.

The following examples will serve for better comprehension of the invention. However, it is to be understood that they are not to be deemed limitative in any degree. The process described in the following can also be applied with the same readiness to the Bra-ethyl, 13epropyl or 13B-butyl derivatives as to the 13,8-methyl derivatives.

Example I.Preparation of 3-ethylenedioXy-4,5-

seco-estrane-17,8-01-5-one 900 cc. of toluene, 18 cc. of pyridine, 180 gm. of 3- ethylenedioxy-4,5-seco-A -estrene 17B ol 5 one and 72 gm. of palladized talc containing 2% of palladium, were introduced into a hydrogenation vessel. The vessel was purged and the mixture was agitated under an atmosphere of hydrogen at room temperature. Over a period of 6 hours about 12 liters of hydrogen were absorbed.

Thereafter, the reaction solution was filtered and 180 cc. of water were added thereto. Next, the washing was effected, followed by decanting, first with an aqueous solution of normal sulfuric acid to eliminate the pyridine, then with an aqueous solution of sodium bicarbonate and finally with water until the wash waters were neutral. The toluene phase was dried over magnesium sulfate, concentrated to dryness under reduced pressure, thus obtaining 180 gm. of raw 3-ethylenedioxy 4,5 seco-estrane-17B-ol-5-one. This product was used as such for the next step.

A sample of this product was purified for analysis by recrystallization from isopropyl ether containing 1 part per thousand of pyridine, then from ethyl ether containing 1 part per thousand of pyridine. It had a melting point of 80 to 85 C. and a specific rotation (c.=1% in methanol containing 1% of pyridine), and it possessed the following characteristics:

Analysis.C H O (molecular weight=336.46): Calculated (percent): C, 71.39; H, 9.59. Found (percent): C, 71.2; H, 9.5.

Infrared spectra (in chloroform): Absorption at:

1,704 cm.- carbonyl 3,600 cmr z hydroxyl and CO-C band, characteristic of the ketal function.

This product is not described in the literature.

The 3-ethylenedioxy 4,5 seco-M-estrene-1719-01-5- one, utilized as the starting product in the preceding preparation, was obtained in the course of the process described in French Patent No. 1,364,556.

In an analogous manner, the 3 ethylenedioxy-13B- ethyl-4,5-seco-gonane-17fl-ol-5-one was prepared by starting with 3-ethylenedioxy 13B ethyl 4,5 seco-A gonene-17fl-ol-5-one, having a melting point of 95 to 100 C., this product being obtained in the course of the process described in the French Patent No. 1,476,509. The 3-ethylenedioxy-13fi-ethyl 4,5 seco-gonane-17fi-ol- 5-one is not described in the literature.

Example II.Preparation of 3,5-bis-(ethylendioxy)-4,

5-seco-estrane-17-one Step A: Preparation of 3,5-bis-(ethylendioxy)4,5-secoestrane-17B-ol.Under an inert atmosphere, first 70 gm. of 3-ethyl-enedioxy 4,5 seco estrane 17B-ol-5-one, then 0.35 gm. of paratoluene sulfonic acid were introduced into 350 cc. of methylethyldioxolane. The mixture was agitated for about 15 hours. Thereafter, the reaction mixture was made alkaline with 2.1 cc. of pyridine, agitated for 10 minutes, then 126 cc. of water and 14 cc. of a saturated aqueous solution of sodium bicarbonate were added. The organic phase was separated by decanting and washed with water. The aqueous wash waters were extracted with benzene, which was washed with water, then combined with the organic phase previously isolated and washed. These combined organic phases were dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was taken 10 up in isopropyl ether and concentrated to dryness under reduced pressure. 84 gm. of a raw product were recovered, which was crystallized from isopropyl ether, obtaining 62.7 lgm. of 3,5-bis-(ethylenedioxy)-4,5-seco-estrane The product had a specific rotation [a] =+18 il (c.=1% in methanol containing 1% of pyridine).

By concentration of the mother liquors resulting from the crystallization, a second yield of product was obtained.

A sample of the product was purified for analysis from isopropyl ether containing 1 part per thousand of pyridine. It had a melting point of to C. and a specific rotation [u] =-+19Oi1 (c.=1% in methanol containing 1% of pyridine), and possessed the following characteristics:

A1zalysis.-C H O (molecular weight=380.50): Calculated (percent): C, 69.44; H, 9.53. Found (percent): C, 69.1; H, 9.7.

Infrared spectra (in chloroform):

Absorption at 3,600 cmf z hydroxy and C-O-C band characteristic of the ketal function.

This product is not described in the literature.

Step B: Preparation of 3,5-bis-(ethylenedioxy)-4,5- seco-estrane-17-one.Under an inert atmosphere, 40 gm. of purified 3,5-biS-(ethylenedioxy)-4,5-seco-estrane-17}3-0l were dissolved in a mixture of 400 cc. of toluene and 80 cc. of methylethylketone in a 2-liter vessel equipped with an agitation means and a descending condenser. The solution was brought to boiling point under agitation. Then after distillation had been established, a solution of 14.4 gm. of aluminum isopropylate in 540 cc. of toluene and 720 cc. of methylethylketone was introduced. This addition was effected as follows: The two reactants were introduced simultaneously at regular intervals for about 15 minutes and within a total time of 4 to 5 hours in such a manner that the evaporated solvent volume was proportionately compensated by the addition of the two reactants. Thus, within a space of about 4 to 5 hours, 1,260 cc. of distillate were recovered. The distillation was continued until 80 cc. of distillate were recovered. The reaction mixture was cooled. Next, 36 cc. of water were introduced and the solution was agitated. The precipitated alumina was vacuum filtered. Water was added to the filtrate and the organic solvents were eliminated by stream distillation. The aqueous mixture was cooled and the precipitate formed was vacuum filtered, washed with water and dried. The recovered raw product was crystallized from methanol containing 1 part per thousand of pyridine, thus obtaining 30. 8 gm. of 3,5-bis-(ethylenedioxy)-4,5-seco-estrane-17-one. The product had a melting point of 114 C.

A sample of this product, purified for analysis by crystallization first from isopropyl ether containing 1 part per thousand of pyridine, then from methanol containing 1 part per thousand of pyridine, had a melting point of 114 C. and a specific rotation [a] =-|-75:1.5 (c.=1% in methanol containing 1% of pyridine), and had the following characteristics:

Analysis.C H O (molecular weight=378.49): Calculated (percent): C, 69.81; H, 9.05. Found (percent): C, 69.9; H, 8.9.

Infrared spectra (in chloroform) Absorption at 1,732 cmf z carbonyl and CO-C band characteristic of the ketal function.

This product is not described in the literature.

Example III.Preparation of 3,5 bis (ethylenedioxy) 4,5-seco-estrane-17-one, starting with 4,5-seco-estrane- 17,B-ol-3,5-dione 10 gm. of 4,5-seco-estrane--01-3,S-dione, a product described in French Patent No. 1,432,569, were introduced into 60 cc. of methylethyldioxolane. The mixture was brought to reflux under an inert atmosphere and 1 volume of solvent was distilled therefrom under normal pressure. The mixture was then cooled toward 75 C. and 0.050 gm. of paratoluene sulfonic acid was added. Under a slight vacuum, the mixture was distilled for 3 hours at about 75 C., recovering about 10 cc. of distillate per hour and maintaining the reaction media at a constant volume by the addition of methylethyldioxolane. Thereafter, the methylethyldioxolane was elminated under re duced pressure. The recation media was cooled. 20 cc. of benzene and 0.4 cc. of pyridine were added to the reaction mixture, which was then homogenized and was, after 18 cc. of water and 2 cc. of a saturated solution of sodium bicarbonate had been added, agitated for 10 minutes. The benzenic phase was separated by decanting and washed with water. The aqueous phases were reextracted with benzene. After having been Washed with water, these benzenic re-extracts were combined with the principal benzenic solution. After the addition of one drop of pyridine, the whole of the combined benzenic solutions was concentrated to dryness under reduced pressure. The resultant residue was dissolved in hot ethyl ether. The ether was expelled under vacuum and the crystallizate was dried. 13.27 gm. of raw product were obtained, having a melting point of 90 to 100 C. and a specific rotation [a] =|l8il (c.=l% in methanol containing 1% of pyridine).

This raw product was recrystallized from isopropyl ether containing 1 part per thousand of pyridine, thus obtaining 8.75 gm. of 3,5-bis-(ethylenedioxy)-4,5-secoestrane-17/i-ol, having a melting point of 90 C. to 100 C. with a specific rotation of [a] =+19.5i1 (c.=1% in methanol containing 1% of pyridine). This product was identical to the 3,5-bis-(ethylenedioxy)-4,5- seco-estrane-17/3-ol prepared in Step A of the preceding example. By applying the process described in Step B of the preceding example to this compound, 3,5-bis-(ethylenedioxy)-4,5-secoestrane-l7-one was obtained, which was identical to the product prepared according to Example II.

Example IV.-Preparation of 3,5-bis-(ethylenedioxy)- 4,5-seco-A -estrene-17-one Step A: Preparation of 3,5-bis-(ethylenedioxy)-17,8- benzoyloxy 4,5 A901) estrene Under an atmosphere of nitrogen, 2 gm. of 17fi-benzoyloxy-4,5-seco-A estrene-3,5-dione, having a specific rotation [a] =|43 (c.=1% in methanol), a product described in French Pat. No. 1,243,000, were introduced into 60 cc. of methylethyldioxolane. 0.06 gm. of paratoluene sulfonic acid monohydrate were added thereto, and the reaction mixture was heated under agitation in order to obtain within the space of hours a volume of distillate of about 20 cc. while maintaining the reaction volume constant by the regular addition of methylethyldioxolane. The pH was adjusted to 8.0 by the addition of an aqueous solution of sodium bicarbonate. The organic phase was separated by decanting, washed with water until neutrality was attained and dried. One drop of pyridine was added to the organic phase, which was then distilled to dryness under reduced pressure. Next, ethanol was added to the residue and the mixture was again concentrated to dryness under reduced pressure.

The resultant residue was crystallized from ethanol, thus obtaining 1.6 gm. of 3,5-bis-(ethylenedioxy)-175- benzoy1oxy-4,5-seco-A -esterene. The product had a melting point of 165 to 166 C.

A sample of this product, recrystallized first from isopropyl ether in the presence of pyridine, then from ethanol also in the presence of pyridine, had the following constants:

Melting point=166 to 167 C. Specific rotation=[u] =+23.2 (c.=0.9% in metha- 12 Analysis.C l-I O (molecular weight:482.6): Calculated (percent): C, 72.17; H, 7.93. Found (percent). C, 72.4; H, 8.1.

Ultraviolet spectra (in ethanol):

max. at 230 Kilt-E 14,300 max. at 273 In,u.e=910 max. at 280 m .t-e=720 This product is not described in the literature. Step B: Preparation of 3,5-bis-(ethy1enedioxy)-4,5-

seco-A -estrene-17p-ol.Under an atmosphere of ni trogen, 600 mg. of 3,5-bis-(ethylenedioxy)-17fl-benzoyloxy-4,5-seco-A -estrene were introduced into 19 cc. of a 0.158 N potassium hydroxide solution. The mixture was maintained at reflux for one hour, then concentrated to dryness under reduced pressure. Next, water was added to the mixture, which was then extracted with ether and the extracts were combined. The organic solution obtained was washed with water, dried and concentrated to dryness. After adding isopropyl ether, the solution was crystallized, vacuum filtered and dried. In this manner, 362 mg. of 3,5 bis (ethylenedioxy)-4,5-seco-A -estrene- 175-01 were obtained having a melting point of 130 C.

A sample of this product was purified by crystallization first from isopropyl ether, then from petroleum ether (boiling range=60 to C.). The product had a melting point of 132 C. and a specific rotation [a] =+25.8 (c.=0.7% in methanol) AnaIysis.C H O (molecular weight=378.49): Calculated (percent): C, 69.81; H, 9.05. Found (percent): C, 69.8; H, 9.1.

This product is not described in the literature.

Step C: Preparation of 3,5-bis-(ethylenedioxy)-4,5- seco-A -estrene-l7-one.Within a space of 10 minutes, about 1 gm. of chromic acid, followed by a solution composed of 10 cc. of pyridine and 1 gm. of 3,5-bis-(ethylenedioxy)-4,5-seco-A -estrene-17B-ol were introduced into 10 cc. of pyridine cooled to 0 C. This mixture was allowed to warm to a temperature of 20 C., then agitated for 15 hours at this temperature. Thereafter, the reaction mixture was poured into water and filtered. The aqueous phase was extracted with methylene chloride and the methylene chloride extracts were combined. The organic solution obtained was washed with water and dried, then concentrated to dryness under reduced pressure.

The residue was crystallized from isopropyl ether and 0.665 gm. of 3,5-bis-(ethylenedioxy)-4,5-sec0-A gst rege-U-one was obtained, having a melting point of A sample of this product was purified for analysis by crystallization from isopropyl ether. It had a melting point of 98 C. and a specific rotation [a] =+105 (c.=0.5% in methanol).

Analysis.C H O (molecular weight=376.46): Calculated (percent): C, 70.18; H, 8.56. Found (percent): C, 70.1; H, 8.5.

This product is not described in the literature.

Example V.Preparation of 17a-ethynyl- 19-nor-testosterone Step A: Preparation of 3,5-bis-(ethylenedioxy)-17aethynyl 4,5 seco-estrane 17,8-ol.Under agitation, a stream of acetylene was allowed to bubble through 40 cc. of a sodium tert.-amylate solution in toluene containing 2.28 gm. of sodium per 100 cc. for 2 hours. Thereafter, 5 gm. of 3,5-bis-(ethylenedioxy)-4,5-seco-estrane-17-one (described in Step B of Example II) and 10 cc. of toluene were introduced into the solution of sodium acetylide obtained. The mixture was then agitated for 3 hours and 30 minutes at room temperature while a stream of acetylene was bubbled therethrough. Next, the reaction mixture was cooled to about 15 C. under an inert atmosphere. A solution of 5 gm. of ammonium chloride in 15 cc. of water was introduced. The toluene was distilled under reduced pressure wh le maintaining the volume constant 13 by addition of water, thus obtaining 5.28 gm. of 3,5-bis- (ethylenedioxy) 17oz ethynyl 4,5-seco-estrane-17p-ol. The product had a melting point of 181 to 182 C. and

was utilized as such for the next step.

A sample of this product, purified for analysis by recrystallization from methanol containing 1 part per thousand of pyridine, had a melting point of 183 C. and a specific rotation [a] =30 L2 (c.=1% in methanol containing 1% of pyridine) and possessed the following characteristics:

Analysis.C H 'O (molecular weight=404.52: Calculated (percent): C, 71.25; H, 8.97. Found (percent): C, 71.4; H, 9.0.

Infrared spectra (in chloroform):

Absorption at:

3,300 cmr ethynyl 3,590 cmr' hydroxyl and COC band characteristic of the ketal function.

This product is not described in the literature.

Step B: Preparation of l7a-ethynyl-4,5-seco-estrane- 17B-ol-3,5-dione.-First, 1.5 gm. of 3,5-bis(ethylenedioxy)-17a-ethynyl-4,S-seco-estrane-17,8-01, then 1.5 gm. of citric acid were introduced into .a mixture of 7.5 cc. of toluene, 3 cc. of methanol and 3 cc. of water. Under agitation and an inert atmosphere, the mixture was held at reflux for one hour. Then 15 cc. of water were added thereto. The toluene was concentrated under reduced pressure. The precipitate formed was isolated by being vacuum filtered, washed with water until the wash waters were neutral and dried. Thus, 1.13 gm. of 17a-ethynyl- 4,5-seco-estrane-17B-ol-3,5-dione were obtained. The product had a melting point of 135 to 136 C. and it was utilized as such for the following step.

A sample of this product, purified for analysis by crystallization from ethyl ether, had a melting point of 135 to 136 C. and a specific rotation [a] =50.4 i2 (c.==1% in methanol) and had the following characteristics:

Analysis.C H O (molecular weight=316.42): Calculated (percent): C, 75.91; H, 8.91. Found (percent): C, 76.0; H, 8.9.

Infrared spectra (in chloroform):

Absorption at:

1,703 cm.- carbonyl 3,300 cmf z ethynyl 3,590 cmr hydroxyl This product is not described in the literature.

Step C: Obtention of 17 a-ethynyl-19-nor-testosterone. Under an inert atmosphere, 0.900 gm. of 17a-ethynyl- 4,5-seco-estrane-17;8-ol-3,5-dione were introduced into a mixture of 9 cc. of methanol and 2.7 cc. of methylene chloride. The mixture was agitated for 15 minutes; then 1 cc. of a methanolic solution of sodium methylate, containing 7.8 gm. of sodium per 100 cc. was added, and the reaction mixture was agitated for 5 hours at room temperature. Thereafter, 0.3 cc. of acetic acid and cc. of water were added. Next, the methanol and the methylene chloride were eliminated under reduced pressure, and the precipitate was vacuum filtered. In this way, 0.84 gm. of 17a-ethynyl-19-nor-testosterone were obtained. The product had a melting point of 206 C. and a specific rotation [u] =22.5 (c.=2% in chloroform).

After having been purified, a sample of this product had a melting point of 206.5 to 207 C. and a specific rotation [a] =24i2 (c.=1% in chloroform) and was found to be identical to a sample of 17u-ethynyl-19- nor-testosterone prepared according to a different method.

Step A: Preparation of 3,5-bis-(ethylenedioxy)-17aethyl-4,5-seco-estrane-17,B-ol.30 cc. of toluene and cc. of ethanol containing 0.2% of pyridine were introduced into a hydrogenation vessel, then 3 gm. of 3,5-bis- (ethylenedioxy)-17a-ethynyl-4,5-seco-estrane-175-01 (described in Step A of Example V) and finally 1.2 gm. of palladized talc containing 2% of palladium were added. The apparatus was purged, and the mixture therein was agitated under an atmosphere of hydrogen until the completion of absorption of the latter. Thereafter the reaction mixture was maintained under agitation for 15 minutes and then the reaction suspension was filtered. The filtrate was distilled to dryness under reduced pressure, obtaining 3.22 gm. of raw 3,5-bis-(ethylenedioxy)-17a-ethyl-4,5- seco-estrane-l7fi-ol which product was utilized as such for the next step.

This product is not described in the literature.

Step B: Preparation of 17a-ethyl-4,5-seco-estrane-17B- ol-3,5-dione.2.13 gm. of raw 3,5-bis-(ethylenedioxy)- 17v -ethyl-4,5-seco-estrane-176-01 were dissolved in a mixture of 107 cc. of toluene, 4.3 cc. of methanol and 4.3 cc. of water. The solution was heated to reflux and 2.13 gm. of citric acid monohydrate were added. Then the solution was maintained at reflux for one hour; thereafter 10.7 cc. of water were added. Next, the solution was concentrated under reduced pressure in order to eliminate the toluene and the methanol. The product obtained was extracted with methylene chloride. The methylene chloride solution was dried over magnesium sulfate, distilled to dryness under vacuum, thereby obtaining 1.55 gm. of raw 17a-ethyl 4,5 seco-estrane-17fl-ol-3,5-dione, which was utilized as such for the next step.

Infrared spectra (in chloroform):

Absorption at:

]J-CH;\

1,708 cm.- carbonyl 3,600 cmr z hydroxyl This product is not described in the literature:

Step C: Obtention of 7u-ethyl-19-nor-testosterone. 1.35 gm. of 17a-ethyl-4,5-seco-estrane-17fi-ol-3,5-dione were dissolved in 7 cc. of methanol, and 0.36 gm. of sodium methylate were added thereto. Next, the solution was agitated for 5 hours at room temperature and thereafter neutralized by the addition of acetic acid. The methanol was distilled therefrom under reduced pressure. Water was added and the insoluble portion of the reaction mixture was extracted with methylene chloride. The methylene chloride solution was dried over magnesium sulfate and concentrated to dryness under reduced pressure. The resultant residue was purified by trituration with ethyl ether, and 0.557 gm. of 17a-ethy1-19-nortestosterone was obtained. The product had a melting point of 136 C. and a specific rotation of [a] =+21i0.5 (c.=2% in methanol).

Ultraviolet spectra (in ethanol) max. at 240 to 241 In,ue=16,45-0

This product was identical to 17a-ethyl-19-nor-test0sterone prepared according to a different method.

Example VII.--Preparation of the acetate of 17aethynyl-19-nor-testosterone Step A: Preparation of 3,5-bis-(ethylenedioxy)-17aethynyl-1713-acetoxy-4,5-seco-estrane.-4 gm. of 3,5-bis- (ethylenedioxy)17u-ethynyl-4,5-seco-estrane-1713-01 (described in Step A of Example V) were introduced into a mixture of 8 cc. of pyridine and 4 cc. of acetic acid anhydride and heated at to C. for 24 hours. Thereafter, the reaction solution was poured into a waterice mixture. The precipitate formed was vacuum filtered, washed with water and dried. This raw product was purified by trituration with methanol. The product obtained after purification with methanol was dissolved in methylene chloride and agitated with magnesium silicate. The methylene chIoride solution was filtered and concentrated 15 to dryness under reduced pressure, thereby obtaining 3.53 gm. of 3,5-bis-(ethylenedioxy)-l7a-ethynyl-17/3-acetoxy- 4,5-seco-estrane. The product had a melting point of 174 C. and was utilized as such for the next step.

A sample of this product, purified for analysis by crystallization from methanol, had a melting point of 174 C. and a specific rotation [a] =31.5- L1 (c.=1% in chloroform containing 1% of pyridine) and possessed the following characteristics:

Analysis.C H O (molecular weight=446.56): Calculated (percent): C, 69.92; H, 8.59. Found (percent): C, 69.9; H, 8.8.

Infrared spectra (in chloroform):

Absorption at:

1,738 cm. carbonyl 3,3 cmr z ethynyl This product is not described in the literature.

Step B: Preparation of l7a-ethynyl-17B-acetoxy-4,5- seco-estrane-3,5-dione.3.2 gm. of 3,5-bis-(ethylenedioxy)-17a-ethynyl-17,8-acetoxy-4,S-seco-estrane were introduced into a mixture of 16 cc. of toluene, 6.4 cc. of methanol and 6.4 cc. of water. Then the reaction mixture was heated to reflux, 3.2 gm. of citric acid monohydrate were added, and the reaction mixture was maintained at reflux for 15 hours. Thereafter, 16 cc. of water were added to the reaction mixture, which was then distilled under reduced pressure in order to eliminate the toluene and the methanol. After the precipitate obtained had been vacuum filtered and dried, 2.58 gm. of a product were recovered which, after crystallization from methanol, supplied 2.2 gm. of 17a ethynyl 17B acetoxy 4,5 seco estrane- 3,5-dione. The product had a melting point of 170 C. and it was utilized as such for the next step.

A sample of this product, purified for analysis by crystallization from methanol, had a melting point of 170 C. and a specific rotation of [a] =59 (c.=1% in chloroform) and showed the following characteristics:

Analysis.--C H O (molecular weight=358.46): Calculated (percent): C, 73.71; H, 8.43. Found (percent): C, 73.4; H, 8.3.

Infrared spectra (in chloroform) Absorption at:

1,708 cmf z carbonyl 1,738 cmf z carbonyl of the acetate 3,300 cmf z ethynyl This product is not described in the literature.

Step C: Preparation of the 3-pyrrolidyl-l7m-ethynyl- 17,6-acetoxy-A -estradiene.--0.500 gm. of 17a-ethnyl- 17B-acetoxy-4,5-seco-estrane-3,5-dione were introduced into cc. of methanol; then 0.25 cc. of pyrrolidine were added. The mixture was agitated for hours at room temperature and under an atmosphere of nitrogen. The precipitate formed was vacuum filtered and washed with methanol, thus obtaining 0.52 gm. of 3-pyrrolidyl-17aethynyl-17,8-acetoxy-A -estradiene. The product had a melting point of 186 C. and a specific rotation [a] =-276i4 (c.=0.5% in dimethylformamide). It was utilized as such for the next step.

Analysis.C H O N (molecular weight=393.55): Calculated (percent): C, 79.34; H, 8.96; N, 3.56. Found (percent): C, 79.1; H, 9.2; N, 3.9.

This product is not described in the literature.

Step D: Preparation of the acetate of l7a-ethynyl-19- nor-testosterone.0.285 gm. of 3-pyrrilidyl-l7a-ethynyl- 17/3-acetoxy-A -estradiene were introduced into 1.4 cc. of 2 N sulfuric acid. The mixture was agitated for 15 hours at room temperature; then it was slowly poured into a mixture of 2.8 cc. of 2 N sodium hydroxide solution and 5.7 gm. of water and ice. Next, the reaction mixture was again agitated for 2 hours at 0 C., acidified with 9 N sulfuric acid to obtain a pH of 1. and then again agitated for one hour at 0 C. The precipitate formed was vacuum filtered, washed with water and dried. This product was twice recrystallized from a water-acetone mixture. 0.154 gm. of acetate of 17a-ethynyl-19- nor-testosterone was obtained. The product had a melting point of 163 C. and a specific rotation (c.=1% in chloroform). It was identical to a sample of the acetate of 17a-ethynyl-19-nor-testosterone prepared according to a different process.

Example VIII.Preparation of 17a-ethynylA estradiene-l7B-ol-3-one Step A: Preparation of 3,5 bis-(ethylenedioxy)-l7aethynyl 4,5 secoA -estrene-17,8-ol.Under an atmosphere of nitrogen, 2.6 gm. of potassium were introduced into a mixture of 26.4 cc. of tert.-amyl alcohol and 10.4 cc. of benzene. The mixture was heated to 55 C. to 60 C. and maintained at this temperature for one hour while agitating. Then a stream of acetylene was allowed to bubble through the reaction solution for one hour and minutes at a temperature of to C. Thereafter, the reaction solution was cooled to room temperature and, while maintaining the bubbling of acetylene therethrough, a solution of 500 mg. of 3,5-bis-(ethylenedioxy) 4,5-seco-A -estrene-l7-one (described in Step C of Example IV) in a mixture of 10.4 cc. of benzene and 10.4 cc. of ethyl ether was introduced into the reaction solution. The reaction mixture was then agitated for two hours while acetylene continued to be bubbled there through. Next, water was added to the reaction mixture. The organic phase was separated by decanting, washed with water, dried and concentrated to dryness under reduced pressure.

The residue was triturated with isopropyl ether and then crystallized from the same solvent. In this manner 350 mg. of 3,5-bis-(ethylenedioxy)-l7a-ethynyl-4,5- seco-A -estrene-17/3-01 were obtained, having a melting point of 152 C.

A sample of this product was purified for analysis by crystallization first from isopropyl ether, then from aqueous methanol. The product had a melting point of 152 C. with a specific rotation [u] =21.5 (c.=0.5% in methanol).

Analysis.C H O (molecular weight=402.51): Calculated (percent): C, 71.61; H, 8.51. Found (percent): C, 7l.5; H, 8.4.

This product is not described in the literature.

Step B: Preparation of 17a-ethynyl-4,5-seco-A -estrene- 17B-ol-3,5-dione.Under an atmosphere of nitrogen, 6 gm. of 3,5-bis-(ethylenedioxy) 17a-ethynyl 4,5-seco- A -estrene-17B-ol were introduced into a mixture of 30 cc. of toluene and 12 cc. of methanol. Then 12 cc. of water are added to the mixture, which was then brought to reflux while agitating. 6 gm. of citric acid were added and the reaction mixture was maintained at reflux for one hour. Thereafter, 30 cc. of water were added and the methanol and toluene were eliminated under reduced pressure. The aqueous phase was extracted with methylene chloride. The extracts were combined and the organic solution obtained was washed with water, dried and finally concentrated to dryness under reduced pressure.

The residue was admixed with ether. The precipitate formed was isolated by being vacuum filtered, and the mother liquors, which will be referred to hereinafter as Solution A, were preserved. The product obtained was purified by crystallization from ether and 0.99 gm. of 17a-etl1ynyl-4,5-seco-A -estrene-17fi-ol-3,5-dione was obtained having a melting point of 124 C.

A sample of this product was recrystallized from ether and had a melting point of 124 C. with a specific rotation [a] :-73 (c.=0.65% in methanol).

A at 248 to 249 In -6:15pm

This product is not described in the literature.

Moreover, by starting with the Solution A maintained at C. for several hours, a precipitate was obtained. This precipitate was vacuum filtered and purified by crystallization from ethyl ether. In this manner, 210 mg. of 17a ethyny1-4,5-seco-A -estrene-17B-3,5-dione were obtained. The product had a melting point of 143 C. and a specified rotation [a] =15 (c.=0.55% in methanol).

Analysis.-C I-I O (molecular weight=314.41); Calculated (percent): C, 76.40; H, 8.33. Found (percent): C, 76.4; H, 8.2.

By employing the conventional processes of ketalization, this compound was converted into 3,5-bis-(ethylenedioxy) 17a ethynyl-4,5-seco-A -estrene-175-01, which could be utilized again.

This product is not described in the literature.

Step C: Preparation of 17tx-ethynyl A estradiene- 17fl-ol-3-one.-Under an inert atmosphere, 0.600 gm. of 1700 ethynyl-4,5-seco-A -estrene-17B-ol-3,5-dione was introduced into 2.2 cc. of benzene. Then, while maintaining the temperature between 0 C. and +3 'C., 1.4 cc. of a solution of sodium tert.-amylate in toluene, containing 2.45 gm. of sodium per 100 cc., was added in the space of 20 minutes. While maintaining the previously recited temperature, the reaction mixture was agitated for 2 hours. Thereafter, first 1 cc. of benzene, then a mixture of 0.3 cc. of tert.-butyl alcohol and 0.5 cc. of benzene were added to the reaction mixture. The temperature was elevated to 20 C. and the reaction mixture was agitated for one hour at this temperature. The pH was adjusted to 7 by the addition of a benzenic solution of acetic acid. Next, the reaction mixture was agitated for 45 minutes and then water was added. The solvents were eliminated under reduced pressure. The precipitate formed was vacuum filtered, washed and dried. 570 mg. of product were obtained, having a melting point of 178 C.

This product was purified by crystallization from ethyl acetate, thus obtaining 416 mg. of 17a-ethynyl-A -estradiene-l7fl-ol-3-one. The product had a melting point of 183 C. and a specific rotation [a] =355 (c.=0.2% in methanol).

Ultraviolet spectra (in ethanol) Infiection toward 235 to 236 m,ue 4,590 Inflection toward 247 In,u.e=3,55O

max. at 304 mp.e= 20,000

Example IX.Preparation of l9-nor-A -pregnene- 160L,170L-dlOl-3,20-dl0[16 Step A: Preparation of 3,5-bis-(ethylenedioxy)-17B- cyano-4,5-seco-estrane-17a-ol.500 gm. of 3,5-bis-(ethylenedioxy)-4,5-seco-estrane-17-one (described in Step B of Example II) were dissolved in liters of methanol; then 860 gm. of potassium cyanide were introduced therein. Next, within the space of about one hour, 600 cc. of acetic acid were added and the reaction mixture was agitated for 18 hours at room temperature. Thereafter, 300 cc. of acetic acid and 10 liters of water were introduced into the reaction mixture, which was then agitated for 3 hours. The precipitate formed was isolated by being vacuum filtered and dried.

This raw product was purified by crystallization from ethyl ether, thus obtaining 259.5 gm. of 3,5-bis-(ethylenedioxy)-17fl-cyano-4,S-seco-estrane-17e-ol, having a melt ing point of 145 C. and a specific rotation [a] :+3O (c.=l% in methanol containing 1% of pyridine).

18 Analysis.C I-I O N (molecular weight=405.52): Calculated (percent): C, 68.12; H, 8.7; N, 3.45. Found (percent): C, 68; H, 8.7; N, 3.6.

This product is not described in the literature.

RECOVERY OF THE STARTING PRODUCT (a) 1 kg. of potassium hydroxide was introduced into the raw methanolic mother liquors. The mixture was agitated for 15 minutes. Then 10 liters of water were added and the reaction mixture was agitated for 20 hours. Thereafter, the precipitate formed was isolated by filtration, washed and dried. In this way, 210 gm. of 3,5-bis- (ethylenedioxy)-4,5-seco-estrane-17-one were recovered, having a melting point of 114 C. and a specific rotation [a] =-|-75 (c.=1% in methanol containing 1% of pyridine), identical to the starting product.

(b) The mother liquors of the crystallization from ether were concentrated to dryness. The residue obtained was purified by chromatography through alumina, then crystallized in ether, obtaining a further yield of 3,5-bis- (ethylenedioxy)-17u-cyano-4,5 seco-estrane-17fi-ol, having a melting point of 145 C. and a specific rotation [a] =--17.5 (c.=1% in methanol containing 1% in pyridine).

Analysis.-C H O N (molecular weight=405.52): Calculated (percent): C, 68.12; H, 8.7; N, 3.45. Found (percent): C, 68.4; H, 8.7; N, 3.7.

This product is not described in the literature.

By adding potassium hydroxide in hydromethanolic medium, this product leads to 3,5-bis-(ethylenedioxy)- 4,5-seco-estrane-17-one, which could be again used for the same preparation.

Step 13: Preparation of 3,5 bis (ethylenedioxy)-17- cyano-4,5-seco-A -estrene.At room temperature, 20 gm. of 3,5 bis (ethylenedioxy) 17,8 cyano-4,5-secoestrane-17ot-ol, with a specific rotation [a] =+33 (c.-=1% in methanol containing 1% of pyridine), were dissolved in cc. of pyridine. Within about 15 minutes, 20 cc. of thionyl chloride were added and the mixture was agitated over a period of 20 hours. Thereafter, the reaction mixture was poured into a water-ice mixture containing 40 gm. of sodium carbonate. Ethyl ether was added thereto and the reaction mixture was again agitated. Then the precipitate formed was eliminated by filtration. The ethereal phase in the filtrate obtained was separated by decanting. The aqueous phase was extracted with ethyl ether and the ethereal phases were combined. The ethereal solution obtained was washed, successively, first with water, then with an aqueous solution of sodium bicarbonate and again with water. The ethereal solution was dried, then concentrated to dryness.

The residue, washed with isopropyl ether, was recrystallized from methanol containing 1 part per thousand of pyridine, thus obtaining 8 gm. of 3,5-bis-(ethylenedioxy)-17-cyano-4,5-seco-A -estrene. The product had a melting point of C. and a specific rotation [061 +35 (c.=l% in methanol containing 1 part per thousand of pyridine).

A sample of this product was recrystallized from methanol containing 1 part per thousand of pyridine.

Analysis.-C H O N (molecular weight-:387.49): Calculated (percent): C, 71.28; H, 8.58; N, 3.61. Found (percent): C, 71.1; H, 8.5; N, 3.8.

Ultraviolet spectra (in ethanol):

max. at 217 to 218 mus=7,960 max. at 264 m .-e=35 This product is not described in the literature.

The sulfite of bis-(3,5-bis-[ethylenedioxy]-17fi-cyano 4,5-seco-estrane-l7et-ol) could be isolated in the following manner. 5 gm. of 3,5-bis-(ethylenedioxy)-17/3-cyano- 4,5-seco-estrane-l7u-ol were dissolved in 20 cc. of pyridine at room temperature. Then within two minutes 0.5 cc. of thionyl chloride were added and the mixture was agitated for one hour at room temperature. Thereafter the reaction mixture was poured into a water-ice mixture containing gm. of sodium carbonate. The sulfite crystallized. It was vacuum filtered, washed to neutrality and dried, thus obtaining the raw sulfite which was then recrystallized from acetone. In this manner, 3.3 gm. of sulfite were recovered, having a melting point of 212 C. with a specific rotation of [a] =+37 (C=0.5% in chloroform containing 1 part per thousand of pyridine).

Analysis.C O I-I SN (molecular weight=857.09): Calculated (percent): C, 64.45; H, 8.0; O, 20.53; N, 3.27; S, 3.74. Found (percent): C, 64.5; H, 7.8; O, 20.7; N, 3.4; S, 4.

This product is not described in the literature.

Subjected to the action of thionyl chloride in pyridine, this sulfite leads to 3,5-bis-(ethylenedioxy)-17-cyano-4,5- seco-A -estrene which could be used again.

Step C: Preparation of 4,5-seco-19-nor-A -pregnene- 3,5,20-trione.-Under an inert atmosphere and within the period of about 20 minutes, a solution of 33 gm. of 3,5- bis-(ethylenedioxy)-17-cyano-4,5-seco-A -estrene in 100 cc. of benzene was introduced into 300 cc. of a methyl lithium solution in ethyl ether containing 1.35 mols/liter. This mixture was agitated for 30 minutes at room temperature. The reaction solution, containing 3,5-bis-(ethylenedioxy)-20-imino 4,5 sec-19-nor-A -pregnene, was poured within a period of about minutes into an acetic acid-water-ice mixture. The organic phase was separated by decanting. The benzene and the ether were eliminated by distillation. Then the solution obtained was maintained for 2 hours at 95 C. Thereafter, it was mixed with benzene and water. The organic phase Was separated by decanting. The aqueous phase was extracted with benzene, and the benzenic extracts were combined. The organic solution obtained was washed successively with water, with an aqueous solution of sodium bicarbonate and again with water. The benzenic solution was dried, then concentrated to dryness under vacuum.

Thus, 27.35 gm. of 4,5-seco-19-nor-A -pregnene-3,5,20- trione were obtained, which product was utilized as such for the next step.

This product is not described in the literature.

Step D: Preparation of 3-pyrrolidyl-19-nor-A -pregnatriene-20-one.-Under an atmosphere of nitrogen, 27 gm. of 4,5-seco-19-nor-A -pregnene-3,5,2O-trione were introduced into 162 cc. of methanol. Then the mixture was filtered to obtain a clear solution. Next, 10.8 cc. of pyrrolidine were added and the mixture Was agitated for 30 minutes at room temperature. The precipitate formed was isolated by filtration, washed and dried.

This raw product was purified by trituration in dimethylformamide, thus obtaining 14.26 gm. of 3-pyrro1idyl- 19-nor-A -pregnatriene-2O-one with a melting point of 174 to 175 C.

A sample of this product was purified by recrystallization from dimethylformamide. A product was obtained having a melting point of 175 C. and a specific rotation [a] =l77i3.5 (c. =0.5% in dimethylformamide).

Analysis.C 4H ON (molecular weight=351.5): Calculated (percent): C, 82.01; H, 9.46; N, 3.98. Found (percent): C, 82; H, 9.3; N, 4.2.

This product is not described in the literature.

Step B: Preparation of 19-nor-A -pregnadiene-3,20- dione.Under an atmopshere of nitrogen and at a temperature of 50 C., 14.2 gm. of 3-pyrrolidyl-19nor-A pregnatriene-ZO-one were introduced into 142 cc. of an aqueous 2 N sulfuric acid solution. The mixture was agitated for 15 minutes at 50 C., then 5 hours at room temperature. Thereafter, the precipitate formed was elimi nated by filtration, and the filtrate was poured under agitation within a period of about one hour into 213 cc. of an aqueous 2 N sodium hydroxide solution. The solution was agitated for 2 hours at 20 C., then acidified to obtain a pH of 2 by the addition of a dilute aqueous sulfuric acid solution, and again agitated. The precipitate formed was isolated by filtration, washed and dried.

This raw product was purified by crystallization from methanol thus obtaining 8.80 gm. of 19-nor-A -pregnadiene-3,20-dione. The product had a melting point of 181 C. and was utilized as such for the next step.

A sample of this product was purified by recrystallization from methanol and had a melting point of 182 C. and a specific rotation [a] =+ll6i2 (c.=l% in methanol).

Analysis.-C H ,-O (molecular weight=298.41): Calculated (percent): C, 80.49; H, 8.78. Found (percent): C, 80.5; H, 8.7.

Ultraviolet spectra (in ethanol):

max. at 240 mne=26,850

This product is not described in the literature.

Step F: Preparation of l9-nor-A -pregnene-16a,17adiol-3,20-dione.-8.475 gm. of 19-nor-A -pregnadiene- 3,20-dione were dissolved in a mixture of 203 cc. of acetone and 16.9 cc. of water. Next, 2.1 cc. of formic acid and then at a temperature of 20 C. within a period of about 30 minutes, a solution of 5.5 gm. of potassium permanganate in a mixture of 106 cc. of acetone and 42.5 cc. of water were introduced therein. Thereafter, a solution of 8 gm. of sodium metabisulfite in 31.5 cc. of water was added to the reaction mixture. The acetone was eliminated by distillation under vacuum. The reaction mixture was cooled to 20 C. and a mixture of 9 cc. of an aqueous solution of 22 B. hydrochloric acid and of 8.5 cc. of water was introduced into the reaction mixture, which was then agitated for 30 minutes. The precipitate formed was vacuum filtered, washed and dried.

In this manner, 7.25 gm. of 19-nor-A -pregnene-16a, l7a-diol-3,20-dione were obtained.

A sample of this product was purified by crystallization from acetone, then from ethyl acetate and had the following characteristics:

Melting point, determined on the Maquenne block:

(1) to C. (2) 200 to 205 C. Specific rotation [a] =-|-32 (c.=1% in methanol) Analysis.-C H O (molecular weight=332.42): Calculated (percent): C, 72.25; H, 8.49. Found (percent): C, 72.3; H, 8.5.

Ultraviolet spectra:

A 240 m,ue=17,500

The 19-nor-A -pregnene-16u,17a-diol-3,20-dione could be converted into 16a,17m-isopropylidenedioxy-19-nor-A pregnene-3,20-dione in the following manner:

1 gm. of 19-nor-A -pregnene-16a-diol-3,20-dione, then 0.04 cc. of an aqueous solution of 55 B. perchloric acid were introduced into 10 cc. of acetone. The mixture was heated to and maintained at reflux for 30 minutes. Next, the reaction mixture was agitated for one hour and 30 minutes at a temperature of 30 C. The pH was adjusted to about 8.0 by the addition of an aqueous solution of sodium bicarbonate, and 10 cc. of Water were added. The precipitate formed was vacuum filtered, Washed and dried.

The raw product obtained was purified by crystallization from acetone, thus obtaining 0.710 gm. of 160:,17ocisopropylidenedioxy-19-nor-A -pregnene-3,20 dione, with a melting point of 228 C.

A sample of this product was purified by a second crystallization from acetone, and had a melting point of 228 C., and a specific rotation [0c] =|88 (c.=1% in chloroform).

Analysis.C H O (molecular weight=372.49): Calculated '(percent): C, 74.15; H, 8.66. Found (percent): C, 74.3; H, 8.7.

Ultraviolet spectra (in ethanol): max. at 240 m .e=l7,400

The preceding specific embodiments are illustrative of the process of the invention. It is to be understood, however, that other expedients known to those skilled in the 21 art can be employed without departing from the spirit of the invention.

We claim: 1. 3,5-diketals of 4,5-seco-gonane-3,5,17-triones of the formula wherein R represents an alkyl having from 1 to 4 carbon atoms; X represents a member selected from the group consisting of wherein R" is lower alkyl and R' is selected from the group consisting of lower alkylene and (6-methylbenzyl)- ethylene; and A is selected from the group consisting of two hydrogens and a double bond.

References Cited UNITED STATES PATENTS 1/1964 Nomine et a1 260340.9

3,164,611 1/1965 Sarett 260340.9

FOREIGN PATENTS 1,003,086 9/1965 Great Britain 260-340.9

ALEX MAZEL, Primary Examiner JAMES H. TURNIPSEED, Assistant Examiner US. Cl. X.R. 

